Catherine Jay

Catherine Jay Email and Phone Number

Clinical Research Associate at Caris Life Sciences @ Caris Life Sciences
Denver, CO, US
Catherine Jay's Location
Denver Metropolitan Area, United States, United States
Catherine Jay's Contact Details

Catherine Jay work email

Catherine Jay personal email

About Catherine Jay

I am a knowledgeable SOCRA Certified Clinical Research Professional with 10+ years of experience and expertise coordinating, monitoring, and auditing Phase 1-3 clinical trials. My capacity to collect and manage data, ensure quality, and improve processes pair well with my ability to communicate effectively with stakeholders of diverse ranks during face-to-face, group, and presentation settings along with my instinct for organizing and motivating others to achieve goals on time and with excellence. Along with my experience, my database knowledge is significant as I am proficient in REDCap, iMedNet, Medidata Rave, InForm, Oracle, and Microsoft Access.My core skills include but are not limited to: GCP/FDA/ICH Regulations, Clinical Research SOPsStakeholder Communication, Data Collection & Management, Quality Assurance, Process Improvement, Report Writing & Editing, Team Collaboration, Speaking & Presentations, Technical Acumen, Critical Thinking, and Problem Solving.

Catherine Jay's Current Company Details
Caris Life Sciences

Caris Life Sciences

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Clinical Research Associate at Caris Life Sciences
Denver, CO, US
Employees:
1477
Catherine Jay Work Experience Details
  • Caris Life Sciences
    Caris Life Sciences
    Denver, Co, Us
  • Caris Life Sciences
    Clinical Research Associate Ii
    Caris Life Sciences Jun 2022 - Present
    Irving, Texas, Us
  • Caris Life Sciences
    Clinical Research Associate
    Caris Life Sciences Jun 2020 - Present
    Irving, Texas, Us
    In my current role as Clinical Research Associate I conduct the initiation, monitoring, and closeout of research sites, utilizing established protocols and SOPs to guide the process. I maintain collaborative and effective communication with personnel at partner sites including coordinators, clinical research physicians, and other staff. My position also involves verifying investigator qualifications, training, and resources along with verification of medical record and research source documentation against case report form data. Central to this role is the reliable, clear, and timely documentation and communication of protocol deviations (from SOPs, GCP, and applicable regulatory requirements) as well as the review of regulatory documents and the completion of monitoring reports.
  • Surgone, Pc
    Clinical Research Manager - Colorado Pelvic Floor Consultants
    Surgone, Pc May 2018 - Jun 2020
    Englewood, Colorado, Us
    I oversaw all research initiatives for the practice, including attaining and dispersing grant funding, acquiring IRB approvals, and overseeing publication of study results. I continually leverage my database building and management expertise to effectively collect and organize study data, reporting results to all stakeholders in a clear and timely manner. In addition, I collaborated with researchers on new IIT protocols and consent forms as well as manage all budgetary aspects of research, patient communication, and correct source documentation.
  • University Of Colorado Anschutz Medical Campus
    Clinical Research Auditor
    University Of Colorado Anschutz Medical Campus Dec 2016 - May 2018
    Aurora, Co, Us
    As an Auditor, I collaborated with fellow Data & Safety Monitoring Committee members to verify safety and ethical treatment of research subjects and ensure all data collected is accurate, valid, and organized. I assisted with processes of identifying, developing and providing instructional activities for investigators to improve knowledge of and compliance with clinical trials management standards. I oversaw QA/DSM within the CU Cancer Center, reviewing and tracking all serious adverse events (SAEs), unanticipated problems (UAPs), and other reportable adverse events (AEs) as well as organized, prepared, and presented reports to the CU Cancer Center Executive Committee and the Colorado Multiple Institutional Review Board (COMIRB).
  • University Of Colorado Anschutz Medical Campus
    Clinical Data Manager
    University Of Colorado Anschutz Medical Campus Sep 2011 - Nov 2016
    Aurora, Co, Us
    In this role, I conducted weekly, monthly, and annual internal audits of inpatient and outpatient transplants for CU Cancer Center’s Bone Marrow Transplant/Hematologic Malignancies Program. I collaborated with our Quality Manager and other stakeholders to organize and report trial data, ensuringeffective coordination, timeliness, and a commitment to quality. I collected and entered data into federally-mandated NMDP database, working with fellow BMT team members and external personnel to rectify all queries, problems, and issues for compliance. I also prepared research team for clinical trial inspections, working with team of fellow quality assurance personnel to establish and present criteria meant to inform successful trial procedures. Medidata Rave, RedCap, iMedNet, and other databases were used consistently to complete my work.
  • Ppd
    Senior Research Study Coordinator
    Ppd Jan 2007 - Jun 2010
    Wilmington, Nc, Us
    In my position as Senior Research Study Coordinator with PPD, I completed pre-study preparation, including facilitating Informed Consent Sessions, and assured quality data capture while monitoring subject safety and understanding during study process. I trained, supervised, and mentored team recruiters, clinical data associates, and research coordinators, communicating and motivate to successfully complete clinical trials.I received two promotions during tenure, in part due to my ability to lead teams that functioned with aneye for quality and efficiency and to my capacity to manage multiple projects effectively.

Catherine Jay Skills

Clinical Research Research Clinical Trials Data Analysis Irb Healthcare Ich Gcp Infectious Diseases Quality Assurance Hospitals Gcp Community Outreach Protocol Ctms Clinical Monitoring Auditing Powerpoint Public Speaking Customer Service Management Microsoft Excel Microsoft Office Team Building Socra Speaking Interpersonal Communication Written Communication Training Emotional Intelligence

Catherine Jay Education Details

  • University Of Iowa
    University Of Iowa
    Genetics And Biotechnology

Frequently Asked Questions about Catherine Jay

What company does Catherine Jay work for?

Catherine Jay works for Caris Life Sciences

What is Catherine Jay's role at the current company?

Catherine Jay's current role is Clinical Research Associate at Caris Life Sciences.

What is Catherine Jay's email address?

Catherine Jay's email address is ca****@****ail.com

What schools did Catherine Jay attend?

Catherine Jay attended University Of Iowa.

What skills is Catherine Jay known for?

Catherine Jay has skills like Clinical Research, Research, Clinical Trials, Data Analysis, Irb, Healthcare, Ich Gcp, Infectious Diseases, Quality Assurance, Hospitals, Gcp, Community Outreach.

Who are Catherine Jay's colleagues?

Catherine Jay's colleagues are Peggy Yena, Elizabeth A. Sumner, Xi Wu, Ph.d., Mom Irwin, Kerry Scriber, Ccrp, Adam Stark, Elena Rivers.

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